Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Ana Westenberger

Showing results (1-10 of 73) with videos related to

Pageof 8
Sort By:
Cold Spring Harbor Perspectives in Medicine|February 9, 2012
Genetics of Parkinson's diseaseChristine Klein, Ana Westenberger
Current Neurology and Neuroscience Reports|September 13, 2014
The genetics of primary familial brain calcificationsAna Westenberger, Christine Klein
Cold Spring Harbor Perspectives in Medicine|August 12, 2024
Genetics of Parkinson's Disease: From Causes to TreatmentAna Westenberger, Norbert Brüggemann, Christine Klein
Current Opinion in Neurology|June 4, 2019
Primary familial brain calcifications: genetic and clinical updateAna Westenberger, Alexander Balck, Christine Klein
Journal of Neural Transmission (Vienna, Austria : 1996)|April 20, 2021
The importance of genetic testing for dystonia patients and translational researchJelena Pozojevic, Christian Beetz, Ana Westenberger
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
X-linked dystonia-parkinsonism: over and above a repeat disorderJelena Pozojevic, Joseph Neos Cruz, Ana Westenberger
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Factors influencing reduced penetrance and variable expressivity in X-linked dystonia-parkinsonismJelena Pozojevic, Björn-Hergen von Holt, Ana Westenberger
Brain : a Journal of Neurology|November 25, 2015
The evolving spectrum of PRRT2-associated paroxysmal diseasesDarius Ebrahimi-Fakhari, Afshin Saffari, Ana Westenberger, et al.
BMC Neurology|January 6, 2022
A mixed-ethnicity myoclonus-dystonia patient with a novel SGCE nonsense mutation: a case reportMeliza Angelica J de Leon, Raymond L Rosales, Christine Klein, et al.
JAMA Neurology|February 17, 2015
Primary familial brain calcification with known gene mutations: a systematic review and challenges of phenotypic characterizationVera Tadic, Ana Westenberger, Aloysius Domingo, et al.
Pageof 8

Showing results (1-10 of 73) with videos related to

Sort By:
Pageof 8
Cold Spring Harbor Perspectives in Medicine|February 9, 2012
Genetics of Parkinson's diseaseChristine Klein, Ana Westenberger
Current Neurology and Neuroscience Reports|September 13, 2014
The genetics of primary familial brain calcificationsAna Westenberger, Christine Klein
Cold Spring Harbor Perspectives in Medicine|August 12, 2024
Genetics of Parkinson's Disease: From Causes to TreatmentAna Westenberger, Norbert Brüggemann, Christine Klein
Current Opinion in Neurology|June 4, 2019
Primary familial brain calcifications: genetic and clinical updateAna Westenberger, Alexander Balck, Christine Klein
Journal of Neural Transmission (Vienna, Austria : 1996)|April 20, 2021
The importance of genetic testing for dystonia patients and translational researchJelena Pozojevic, Christian Beetz, Ana Westenberger
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
X-linked dystonia-parkinsonism: over and above a repeat disorderJelena Pozojevic, Joseph Neos Cruz, Ana Westenberger
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Factors influencing reduced penetrance and variable expressivity in X-linked dystonia-parkinsonismJelena Pozojevic, Björn-Hergen von Holt, Ana Westenberger
Brain : a Journal of Neurology|November 25, 2015
The evolving spectrum of PRRT2-associated paroxysmal diseasesDarius Ebrahimi-Fakhari, Afshin Saffari, Ana Westenberger, et al.
BMC Neurology|January 6, 2022
A mixed-ethnicity myoclonus-dystonia patient with a novel SGCE nonsense mutation: a case reportMeliza Angelica J de Leon, Raymond L Rosales, Christine Klein, et al.
JAMA Neurology|February 17, 2015
Primary familial brain calcification with known gene mutations: a systematic review and challenges of phenotypic characterizationVera Tadic, Ana Westenberger, Aloysius Domingo, et al.
Pageof 8